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控制生物静滴的接触角以研究其干燥开裂模式。

Controlling the contact angle of biological sessile drops for study of their desiccated cracking patterns.

作者信息

Chen Ruoyang, Zhang Liyuan, Shen Wei

机构信息

Department of Chemical Engineering, Monash University, Clayton, Victoria 3800, Australia.

出版信息

J Mater Chem B. 2018 Oct 7;6(37):5867-5875. doi: 10.1039/c8tb01979g. Epub 2018 Sep 3.

Abstract

Current exploration of cracking patterns of desiccated biological sessile drops as a new approach of scientific research is progressing rapidly. It has been proposed that biological fluids are naturally capable of storing information. Cracking patterns of desiccated biological sessile drops have the potential to provide a facile means to study the links between compositions of biofluids, their structures and their functions. This potential is, however, limited by our current inability to control the influences of non-pathological factors on cracking patterns. Among the non-pathological factors, the initial sessile drop contact angle has a strong influence on cracking patterns through affecting the material transport and stress distributions within the drop. In this work, we developed a method to control the initial drop contact angle on a glass surface to enable the investigation of the contact angle-induced pattern changes in a biological sessile drop. Human blood was selected as the biofluid in this study, because of its richness in cracking patterns. It has been found that the increase in the initial contact angle enlarges the orthoradial cracks close to the drop edge and compresses the width of the peripheral region. We have also concluded that the number of cracks in the central region of the desiccated pattern can be correlated with the drop contact angle. This work also provides a novel protocol for fabricating standardized substrates for studies of desiccation patterns of biological and other complex colloidal fluids.

摘要

当前,将干燥生物 sessile 液滴的破裂模式作为一种新的科研方法的探索正在迅速发展。有人提出生物流体天然具有存储信息的能力。干燥生物 sessile 液滴的破裂模式有可能提供一种简便的方法来研究生物流体的成分、结构和功能之间的联系。然而,这种潜力受到我们目前无法控制非病理因素对破裂模式影响的限制。在非病理因素中,初始 sessile 液滴接触角通过影响液滴内的物质传输和应力分布,对破裂模式有很大影响。在这项工作中,我们开发了一种方法来控制玻璃表面上的初始液滴接触角,以便研究生物 sessile 液滴中接触角引起的模式变化。在本研究中选择人类血液作为生物流体,因为其具有丰富的破裂模式。已经发现,初始接触角的增加会扩大靠近液滴边缘的径向裂纹,并压缩周边区域的宽度。我们还得出结论,干燥模式中心区域的裂纹数量可以与液滴接触角相关联。这项工作还提供了一种新颖的方案,用于制造标准化的基板以研究生物和其他复杂胶体流体的干燥模式。

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